The single kinin receptor signals to separate and independent physiological pathways in Malpighian tubules of the yellow fever mosquito

Author:

Schepel Stephen A.1,Fox Andrew J.1,Miyauchi Jeremy T.1,Sou Tiffany1,Yang Jason D.1,Lau Kenneth1,Blum Austin W.1,Nicholson Linda K.2,Tiburcy Felix3,Nachman Ronald J.4,Piermarini Peter M.1,Beyenbach Klaus W.1

Affiliation:

1. Departments of 1Biomedical Sciences and

2. Molecular Biology and Genetics, Cornell University, Ithaca, New York;

3. Department of Biology, Division of Animal Physiology, Universität Osnabrück, Osnabrück, Germany; and

4. Southern Plains Agricultural Research Center, Agricultural Research Service, U.S. Department of Agriculture, College Station, Texas

Abstract

In the past, we have used the kinins of the cockroach Leucophaea (the leucokinins) to evaluate the mechanism of diuretic action of kinin peptides in Malpighian tubules of the yellow fever mosquito Aedes aegypti . Now using the kinins of Aedes (the aedeskinins), we have found that in isolated Aedes Malpighian tubules all three aedeskinins (1 μM) significantly 1) increased the rate of fluid secretion (V̇S), 2) hyperpolarized the basolateral membrane voltage (Vbl), and 3) decreased the input resistance (Rin) of principal cells, consistent with the known increase in the Clconductance of the paracellular pathway in Aedes Malpighian tubules. Aedeskinin-III, studied in further detail, significantly increased V̇Swith an EC50of 1.5 × 10−8M. In parallel, the Na+concentration in secreted fluid significantly decreased, and the K+concentration significantly increased. The concentration of Clremained unchanged. While the three aedeskinins triggered effects on Vbl, Rin, and V̇S, synthetic kinin analogs, which contain modifications of the COOH-terminal amide pentapeptide core sequence critical for biological activity, displayed variable effects. For example, kinin analog 1578 significantly stimulated V̇Sbut had no effect on Vbland Rin, whereas kinin analog 1708 had no effect on V̇Sbut significantly affected Vbland Rin. These observations suggest separate signaling pathways activated by kinins. One triggers the electrophysiological response, and the other triggers fluid secretion. It remains to be determined whether the two signaling pathways emanate from a single kinin receptor via agonist-directed signaling or from a differentially glycosylated receptor. Occasionally, Malpighian tubules did not exhibit a detectable response to natural and synthetic kinins. Hypothetically, the expression of the kinin receptor may depend on developmental, nutritional, and/or reproductive signals.

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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